E-LIB Suche - Ergebnisse für: Khani, Marzieh

1

Atypical presentations in an RTD patient and report of nove..:

Sabeghi, Donya ; InanlooRahatloo, Kolsoum ; Mirzadeh, Hanieh S....
Acta Neurologica Belgica. 124 (2024) 4 - p. 1363-1370 , 2024

Link: https://doi.org/10.1007/..

2

Identification of a mutation in TNRC18 in a patient with cl..:

Khani, Marzieh ; Shamshiri, Hosein ; Nafissi, Shahriar...
Clinical Case Reports. 12 (2024) 1 - p. , 2024

Link: https://doi.org/10.1002/..

3

Towards a Global View of Parkinson's Disease Genetics:

Khani, Marzieh ; Cerquera‐Cleves, Catalina ; Kekenadze, Mariam...
Annals of Neurology. 95 (2024) 5 - p. 831-842 , 2024

Link: https://doi.org/10.1002/..

4

Challenge accepted: uncovering the role of rare genetic var..:

Khani, Marzieh ; Gibbons, Elizabeth ; Bras, Jose.
Molecular Neurodegeneration. 17 (2022) 1 - p. , 2022

Link: https://doi.org/10.1186/..

5

Correction: Challenge accepted: Uncovering the role of rare..:

Khani, Marzieh ; Gibbons, Elizabeth ; Bras, Jose.
Molecular Neurodegeneration. 17 (2022) 1 - p. , 2022

Link: https://doi.org/10.1186/..

6

Identification of UBA1 as the causative gene of an X‐linked..:

Khani, Marzieh ; Nafissi, Shahriar ; Shamshiri, Hosein...
European Journal of Neurology. 29 (2022) 12 - p. 3556-3563 , 2022

Link: https://doi.org/10.1111/..

7

BVVL/ FL: features caused by SLC52A3 mutations; WDFY4 and T..:

Khani, Marzieh ; Shamshiri, Hosein ; Taheri, Hanieh...
Neurobiology of Aging. 99 (2021) - p. 102.e1-102.e10 , 2021

Link: https://doi.org/10.1016/..

8

A case of adult onset Sandhoff disease that mimics Brown-Vi..:

Khani, Marzieh ; Shamshiri, Hosein ; Moazzeni, Hamidreza...
Neuromuscular Disorders. 31 (2021) 6 - p. 528-531 , 2021

Link: https://doi.org/10.1016/..

9

Insights into the regulatory molecules involved in glaucoma..:

Moazzeni, Hamidreza ; Khani, Marzieh ; Elahi, Elahe
American Journal of Medical Genetics Part C: Seminars in Medical Genetics. 184 (2020) 3 - p. 782-827 , 2020

Link: https://doi.org/10.1002/..

10

Deep geno- and phenotyping in two consanguineous families w..:

Khani, Marzieh ; Taheri, Hanieh ; Shamshiri, Hosein...
Journal of Neurology. 268 (2020) 2 - p. 640-650 , 2020

Link: https://doi.org/10.1007/..

11

Description of combined ARHSP/JALS phenotype in some patien..:

Khani, Marzieh ; Shamshiri, Hosein ; Fatehi, Farzad...
Molecular Genetics & Genomic Medicine. 8 (2020) 7 - p. , 2020

Link: https://doi.org/10.1002/..

12

Mutation screening of SLC52A3, C19orf12, and TARDBP in Iran..:

Khani, Marzieh ; Alavi, Afagh ; Shamshiri, Hosein...
Neurobiology of Aging. 75 (2019) - p. 225.e9-225.e14 , 2019

Link: https://doi.org/10.1016/..

13

Continuum of phenotypes in hereditary motor and sensory neu..:

Khani, Marzieh ; Taheri, Hanieh ; Shamshiri, Hosein...
American Journal of Medical Genetics Part A. 179 (2019) 8 - p. 1507-1515 , 2019

Link: https://doi.org/10.1002/..

14

Gaussian Charge Distributions for Incorporation of Electros..:

Eslami, Hossein ; Khani, Marzieh ; Müller-Plathe, Florian
Journal of Chemical Theory and Computation. 15 (2019) 7 - p. 4197-4207 , 2019

Link: https://doi.org/10.1021/..

15

Identification of direct target genes of miR-7, miR-9, miR-..:

Moazzeni, Hamidreza ; Najafi, Ali ; Khani, Marzieh
Molecular and Cellular Probes. 34 (2017) - p. 45-52 , 2017

Link: https://doi.org/10.1016/..